Life insurers’ new genetic test policy called an 11th-hour stalling attempt
The decision by Canada’s life insurers to stop requiring genetic testing for the vast majority of new policy holders is
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‘At Risk’ Online Support Forum
The Huntington Society of Canada (HSC) is excited to announce the beginning of a new service: an online support forum.
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‘Every confidence first Huntington disease treatments’ in the works
Robert Pacifici, Ph.D. and chief scientific officer for CHDI, granted an interview about the latest Huntington disease research to Gene
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‘It completely changed my life,’ man says of rare Huntington’s disease diagnosis
Orillia’s The Packet & Times is joined by HSC’s Annie Vanexem and several members of the HD community to discuss
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“Her diagnosis blindsided us.”
What is HD? PSA Guest Post Heath Sterling, 40 June 20, 2016 When I learned that my mom had Huntington
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“Huntington disease is devastating.”
What is HD? PSA Guest Post Lindsay Groot, 29 May 2, 2016 Huntington disease (HD) is devastating. Over time, your
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“I’ve got a whole team on my side”
What is HD? PSA Guest Post Jaclyn Skinner, 27 May 9, 2016 Huntington disease (HD) has always been part of my
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“Now is the most exciting time in the history of HD research.”
What is HD? PSA Guest Post Tam Maiuri, 37 May 23, 2016 My grandfather had Huntington disease (HD), so we have
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“The HD community is a powerful group of people.”
What is HD? PSA Guest Post Rob Laycock, 67 May 30, 2016 My mother was diagnosed with Huntington disease (HD) back
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“Together, we’re going to cure HD.”
What is HD? PSA Guest Post Tim Irwin, 44 May 16, 2016 When my grandfather was going through Huntington disease (HD),
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#cureHD Tie-Dye Campaign Launched with Huntington Society of Canada
By Grant Ivens & Jo Zadorsky June 6, 2016 CEO Bev Heim-Myers rocking her #cureHD shirt at national office! The
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$900,000 Grant Could Lead to Key Pieces of Huntington’s Puzzle
In 2012, the University of Alberta’s Dr. Simonetta Sipione made global headlines when she announced that her lab had
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